谷胱甘肽
过氧亚硝酸盐
氧化应激
化学
NAD+激酶
生物化学
糖尿病
体内
链脲佐菌素
荧光团
药理学
荧光
医学
生物
内分泌学
超氧化物
酶
生物技术
物理
量子力学
作者
Renfeng Jiang,Hongshuai Zhang,Qian Liu,Xuefeng Yang,Longwei He,Lin Yuan,Dan Cheng
标识
DOI:10.1002/adhm.202302466
摘要
Abstract Diabetes and its complications, such as diabetes liver disease, is a major problem puzzling people's health. The detection of redox states in its pathological process can effectively help us gain a deeper understanding of the disease. The pair of oxidation–reduction substances peroxynitrite (ONOO − ) and glutathione (GSH) is considered to be closely related to their occurrence and development. Thus, direct visualization of ONOO − and GSH in diabetes liver disease is critical to evaluate the disease at the molecular level. Herein, two activatable agents NTCF‐ONOO − and NTCF‐GSH are prepared for selectively detecting ONOO − and GSH through protection and deprotection strategies based on hydroxyl and amino groups of near‐infrared fluorophore. Fluorescence imaging of exogenous and endogenous ONOO − and GSH changes in living cells and in vivo is observed. The ONOO − and GSH level in the diabetes liver disease cellular model are visualized and the possible redox imbalance mechanism related to the oxidized (NAD + ) and reduced (NADH) nicotinamide adenine dinucleotides is explored in this process. Moreover, these probes can sensitively recognize ONOO − and GSH in the process of oxidative stress resulting from streptozotocin and streptozotocin/acetaminophen‐induced complex diabetic liver disease in vivo. In addition, they can be applied for monitoring the clinical serum sample related with diabetic patients.
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